US4012840A - Adhesive pit and fissure sealant - Google Patents
Adhesive pit and fissure sealant Download PDFInfo
- Publication number
- US4012840A US4012840A US05/657,585 US65758576A US4012840A US 4012840 A US4012840 A US 4012840A US 65758576 A US65758576 A US 65758576A US 4012840 A US4012840 A US 4012840A
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- US
- United States
- Prior art keywords
- teeth
- cyanoacrylate
- sealing
- fissures
- sealant
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000853 adhesive Substances 0.000 title abstract description 11
- 230000001070 adhesive effect Effects 0.000 title abstract description 11
- 239000000068 pit and fissure sealant Substances 0.000 title abstract description 6
- 239000000463 material Substances 0.000 claims abstract description 41
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 23
- -1 alkyl α-cyanoacrylate Chemical compound 0.000 claims abstract description 14
- 239000002245 particle Substances 0.000 claims abstract description 14
- 235000012239 silicon dioxide Nutrition 0.000 claims abstract description 8
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 8
- 239000000203 mixture Substances 0.000 claims description 16
- 238000007789 sealing Methods 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 12
- GYVGXEWAOAAJEU-UHFFFAOYSA-N n,n,4-trimethylaniline Chemical compound CN(C)C1=CC=C(C)C=C1 GYVGXEWAOAAJEU-UHFFFAOYSA-N 0.000 claims description 6
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 claims description 4
- GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 claims description 4
- 239000011248 coating agent Substances 0.000 claims description 3
- 238000000576 coating method Methods 0.000 claims description 3
- 239000000565 sealant Substances 0.000 description 15
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
- 238000006116 polymerization reaction Methods 0.000 description 11
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 10
- 239000003566 sealing material Substances 0.000 description 8
- FGBJXOREULPLGL-UHFFFAOYSA-N ethyl cyanoacrylate Chemical compound CCOC(=O)C(=C)C#N FGBJXOREULPLGL-UHFFFAOYSA-N 0.000 description 6
- 229910002012 Aerosil® Inorganic materials 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- ZHNUHDYFZUAESO-UHFFFAOYSA-N formamide Substances NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 210000000214 mouth Anatomy 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 208000002925 dental caries Diseases 0.000 description 2
- 210000003298 dental enamel Anatomy 0.000 description 2
- 238000005530 etching Methods 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
- 239000004926 polymethyl methacrylate Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000011343 solid material Substances 0.000 description 2
- BQZJOQXSCSZQPS-UHFFFAOYSA-N 2-methoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OC)C(=O)C1=CC=CC=C1 BQZJOQXSCSZQPS-UHFFFAOYSA-N 0.000 description 1
- AXDJCCTWPBKUKL-UHFFFAOYSA-N 4-[(4-aminophenyl)-(4-imino-3-methylcyclohexa-2,5-dien-1-ylidene)methyl]aniline;hydron;chloride Chemical compound Cl.C1=CC(=N)C(C)=CC1=C(C=1C=CC(N)=CC=1)C1=CC=C(N)C=C1 AXDJCCTWPBKUKL-UHFFFAOYSA-N 0.000 description 1
- 229910002020 Aerosil® OX 50 Inorganic materials 0.000 description 1
- 229910001316 Ag alloy Inorganic materials 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-N Metaphosphoric acid Chemical compound OP(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- MWCLLHOVUTZFKS-UHFFFAOYSA-N Methyl cyanoacrylate Chemical compound COC(=O)C(=C)C#N MWCLLHOVUTZFKS-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical group COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 238000007718 adhesive strength test Methods 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 238000010539 anionic addition polymerization reaction Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000004299 exfoliation Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- YZASAXHKAQYPEH-UHFFFAOYSA-N indium silver Chemical compound [Ag].[In] YZASAXHKAQYPEH-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 238000005325 percolation Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/80—Preparations for artificial teeth, for filling teeth or for capping teeth
- A61K6/884—Preparations for artificial teeth, for filling teeth or for capping teeth comprising natural or synthetic resins
- A61K6/887—Compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
Definitions
- the present invention relates to an adhesive pit and fissure sealant useful in dental practice. More particularly, the present invention relates to an adhesive pit and fissure sealant which is useful in the sealing of pits and fissures of sound teeth to prevent teeth from decaying, and to a method for sealing the same.
- the occlusal surfaces of molars have pits and fissures. Food debris and the like penetrate the pits and fissures which eventually results in dental caries. Recently, attempts have been made to seal pits and fissures for the purpose of preventing dental caries.
- Buonocore also developed a sealant consisting of as major ingredients, three parts by weight of the reaction product of bisphenol A and glycidyl methacrylate and one part by weight of methyl methacrylate monomer in which approximately 2% benzoin methyl ester is dissolved as an ultraviolet light sensitive catalyst (Journal of the American Dental Association, 80, 324, 1970). Further, Takeuchi et al have found a tooth filling material useful for sealing cracks, fissures and cavities consisting of a monomeric lower alkyl ⁇ -cyanoacrylate, such as ethyl ⁇ -cyanoacrylate monomer.
- the monomer is applied to the tooth followed by a second material comprising microfine particles of a dentally acceptable solid material having a particle size of about 3 to 500 microns, which particles may be in admixture coated with lower alkyl methacrylate polymer, such as methacrylate polymer powder.
- the dentally acceptable solid materials include gold, silver, nickel, tin, aluminum, platinum, indium, copper, iron, chromium, stainless steel, brass, indium-silver alloy, porcelain and fibrous or powdery glass (U.S. Pat. No. 3,518,762).
- tooth sealants require simple procedures and short practice times as well as long supporting times.
- the sealing procedure which employs sealants made by Buonocore is complicated and requires long hardening times, i.e., more than 30 seconds.
- the sealants disclosed in Takeuchi's U.S. patent have the disadvantage that adhesion is decreased even when applied to teeth etched with acid.
- one object of the present invention is to provide a new and improved sealant for sealing pits and fissures of sound teeth.
- Another object of the present invention is to provide a method for sealing the pits and fissures of sound teeth.
- an adhesive pit and fissure sealant which consists of a first material of a lower alkyl ⁇ -cyanoacrylate and ultra microfine particles of silicon dioxide, a second material of a di-lower alkylformamide and a third material of a hardening promoter.
- the first material used in the composition of the present invention is a lower alkyl ⁇ -cyanoacrylate, e.g., methyl, ethyl, n-propyl, isopropyl, n-butyl and isobutyl ⁇ -cyanoacrylates. Of these, ethyl ⁇ -cyanoacrylate is particularly preferred.
- the first material also contains ultra microfine particles of silicon dioxide which are available as, for example, Aerosil (Nippon Aerosil, trademark) or white carbon.
- the size of the ultra microfine particles range from 10 to 100 millimicrons and hydrophobic particles are particularly preferred.
- the sizes of the silicon dioxide particles are one thousandth to one ten thousandth of the particle size of the fillers hitherto used in the dental field.
- the smaller size particles result in favorable properties of the sealing material as mentioned below by mixing 1 to 30% by weight, preferably 5 to 10% by weight of the lower alkyl ⁇ -cyanoacrylate.
- the first material formulated possesses thixotropy, and flows and spreads by applying power to the surfaces of the teeth even after the second material is added to initiate polymerization.
- the first material is very important in obtaining the improved results of the present invention.
- the hydrophilic properties of the resulting sealing material are substantially reduced, which increases the water-resisting qualities in oral cavities and prevents the deterioration of teeth.
- Favorable properties, such as the hardness and abrasion-resistant properties, are reinforced with silicon dioxide.
- the material is useful in reducing the residual strain of the resin on hardening and decreases the thermal expansion coefficient in the oral cavities after sealing and thereby relieves the influence of the internal stress of the sealing material. Accordingly, exfoliation, loss or leakage of the sealing material does not occur, and the adhesive strength to the teeth is maintained semipermanently.
- the prior art compositions when the filler having a large particle size is combined with the resin in the sealing material, the abrasion-resistant properties were improved but the resinous properties were spoiled. This disadvantage is improved in the present invention.
- the second material used in this invention is a di-lower alkyl formamide, which may be employed in admixture with the first material just prior to use to initiate polymerization of the lower alkyl ⁇ -cyanoacrylate.
- One to 20 parts, preferably 2 to 10 parts by weight of the di-loweralkyl formamide per 100 parts by weight of the first material is mixed with the first material.
- the thus obtained mixture may be employed within 2 to 3 minutes to 1 to 2 hours after mixing, which time may be controlled according to the amount of di-lower-alkyl formamide in the admixture.
- the polymerization rate may be regulated by adding a very small amount of water to the di-loweralkylformamide or by blowing carbon dioxide into the di-loweralkylformamide.
- Di-loweralkylformamide acts as a catalyst in the anionic polymerization reaction of lower alkyl ⁇ -cyanoacrylate, which progresses slowly. In such slow polymerization, a polymer having a high degree of polymerization is obtained, which has lowered residual strain and elevated flexibility in comparison with polymers obtained by rapid polymerization.
- the shrinkage coefficient of the lower alkyl ⁇ -cyanoacrylate on polymerization is, in general, large, the influence of shrinkage after sealing is decreased in the present invention as contraction, which will occur on polymerization, is produced before sealing by adding a di-loweralkylformamide to the first material prior to sealing to initiate the polymerization. As a result, the sealing of pits and fissures in the teeth, and the adhesive strength between the sealing material and tooth were found to be stable, and the integrity of the seal is maintained for a long time.
- the third material of this invention includes N, N-dimethyl-p-toluidine, N, N-dimethylaniline and N, N-diethylaniline, which are generally dissolved in ethanol, n-hexane or the like.
- the surfaces of the teeth to be treated are prepared by brushing with pumice, etching with acids such as phosphoric acid and citric acid, washing with water and air-dried.
- the mixture of the first and second materials which begins to polymerize is coated on the surfaces of the teeth pretreated as described above, with the tip of a small brush. Since the mixture of materials is thixotropic as mentioned earlier in spite of its high viscosity, homogeneous coating of the desired portions is possible and clinical processability is very excellent.
- the teeth are covered with the mixture.
- the third material is then applied. Hardening of the surface of the sealing material occurs within 10 to 15 seconds and occlusion is made possible. However, in the inner portions of the sealing material, the polymerization proceeds slowly because of the presence of the di-loweralkylformamide and thereby the preferred polymer is obtained. The results obtained are excellent and the tooth surfaces are finely finished. Grinding of the occlusal surfaces is not required, except when the sealing is too high.
- the coated sealant adheres firmly to teeth physically and chemically at the surfaces of the pits and fissures, and does not easily exfoliate, loosen or leak out.
- the adhesive strength of sealant to the enamel of teeth was tested in the following manner. After the labial surface of a bovine tooth was etched with acid, the tooth was coated with a mixture of the first and second materials of the sealant of the present invention. A round stick of Polymethacryl (6 mm diameter) was placed against the coated materials and the third material was applied onto the surface of the materials to harden the composition.
- the coated tooth was immersed in water at 37° C for one week within 5 minutes after applying the third material, and thereafter the tensile strength was measured with a tensile testing machine and the adhesive strength per unit of area was calculated.
- the sealant of this invention adheres extremely well compared to the conventional sealants.
- the processability, water-resisting properties and the hardness of the composition of the present invention are improved by employing the combination of the first, second and third materials.
- sealants having lowered residual strain and great flexibility are obtained as shrinkage on hardening is reduced and internal stress is relieved because of the combination of an ultra-microfine powder of silicon dioxide and the slow starting of the polymerization caused by the di-loweralkylformamide.
- great adhesive strength between the sealants and the enamel is maintained.
- the first material 7 percent Aerosil R 972 is mixed with ethyl ⁇ -cyanoacrylate.
- the second material Dimethylformamide.
- the third material n-Hexane solution containing 2%, N,N-dimethyl-p-toluidine.
- the second material Five percent of the second material was mixed with the first material as described above and then the resulting mixture was allowed to stand for 2 to 10 minutes, during which time the surfaces of the molar teeth of a patient were etched with 3 M phosphoric acid for 30 seconds, and washed with water. Moisture was removed from the teeth by a cotton roll and the teeth were air-dried.
- the mixture of the first and second materials as described above was coated onto the teeth surfaces by the tip of a small brush impregnated with the mixture. The mixture penetrated into the pits and fissures of the teeth. Then the third material was applied onto the teeth surfaces and allowed to stand for 5 to 15 seconds. It took about 2 minutes to treat the patient.
Landscapes
- Health & Medical Sciences (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Plastic & Reconstructive Surgery (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Dental Preparations (AREA)
Abstract
An adhesive pit and fissure sealant for tooth surfaces which consists of a first material of a lower alkyl α-cyanoacrylate and ultra-microfine particles of silicon dioxide, a second material of a di-lower-alkylformamide and a third material of a hardening promoter.
Description
This is a division of application Ser. No. 508,733, filed Sept. 24, 1974 and now abandoned.
1. Field of the Invention
The present invention relates to an adhesive pit and fissure sealant useful in dental practice. More particularly, the present invention relates to an adhesive pit and fissure sealant which is useful in the sealing of pits and fissures of sound teeth to prevent teeth from decaying, and to a method for sealing the same.
2. Description of the Prior Art
The occlusal surfaces of molars have pits and fissures. Food debris and the like penetrate the pits and fissures which eventually results in dental caries. Recently, attempts have been made to seal pits and fissures for the purpose of preventing dental caries.
In an attempt to achieve this purpose Takeuchi et al developed a process to protect sound teeth by coating the teeth with a lower alkyl α-cyanoacrylate over the openings of the pits and fissures. The powder containing PMMA as a base is added thereto and pressed into the pits and fissures which protects the sound teeth (Japanese Pat. No. 689,555). M. G. Buonocore et al have developed a process which comprises etching the surface of teeth with acid and then covering the etched surface with a mixture previously formed from methyl cyanoacrylate and PMMA powder (Journal of the American Dental Association 75, 121, 1967). M. G. Buonocore also developed a sealant consisting of as major ingredients, three parts by weight of the reaction product of bisphenol A and glycidyl methacrylate and one part by weight of methyl methacrylate monomer in which approximately 2% benzoin methyl ester is dissolved as an ultraviolet light sensitive catalyst (Journal of the American Dental Association, 80, 324, 1970). Further, Takeuchi et al have found a tooth filling material useful for sealing cracks, fissures and cavities consisting of a monomeric lower alkyl α-cyanoacrylate, such as ethyl α-cyanoacrylate monomer. The monomer is applied to the tooth followed by a second material comprising microfine particles of a dentally acceptable solid material having a particle size of about 3 to 500 microns, which particles may be in admixture coated with lower alkyl methacrylate polymer, such as methacrylate polymer powder. The dentally acceptable solid materials include gold, silver, nickel, tin, aluminum, platinum, indium, copper, iron, chromium, stainless steel, brass, indium-silver alloy, porcelain and fibrous or powdery glass (U.S. Pat. No. 3,518,762).
As reported by the Committee of the American Dental Association and the Scientific Group of WHO, tooth sealants require simple procedures and short practice times as well as long supporting times. Viewed in this light, the sealing procedure which employs sealants made by Buonocore is complicated and requires long hardening times, i.e., more than 30 seconds, Also, the sealants disclosed in Takeuchi's U.S. patent have the disadvantage that adhesion is decreased even when applied to teeth etched with acid.
A need, therefore, continues to exist for a method of treating dental pits and fissures with a sealing composition by simple procedures and in short practice times.
Accordingly, one object of the present invention is to provide a new and improved sealant for sealing pits and fissures of sound teeth.
Another object of the present invention is to provide a method for sealing the pits and fissures of sound teeth.
Briefly, these objects and other objects of the invention as hereinafter will become more readily apparent can be attained by an adhesive pit and fissure sealant which consists of a first material of a lower alkyl α-cyanoacrylate and ultra microfine particles of silicon dioxide, a second material of a di-lower alkylformamide and a third material of a hardening promoter.
The first material used in the composition of the present invention is a lower alkyl α-cyanoacrylate, e.g., methyl, ethyl, n-propyl, isopropyl, n-butyl and isobutyl α-cyanoacrylates. Of these, ethyl α-cyanoacrylate is particularly preferred.
The first material also contains ultra microfine particles of silicon dioxide which are available as, for example, Aerosil (Nippon Aerosil, trademark) or white carbon. The size of the ultra microfine particles range from 10 to 100 millimicrons and hydrophobic particles are particularly preferred. The sizes of the silicon dioxide particles are one thousandth to one ten thousandth of the particle size of the fillers hitherto used in the dental field. The smaller size particles result in favorable properties of the sealing material as mentioned below by mixing 1 to 30% by weight, preferably 5 to 10% by weight of the lower alkyl α-cyanoacrylate.
The first material formulated possesses thixotropy, and flows and spreads by applying power to the surfaces of the teeth even after the second material is added to initiate polymerization. The first material is very important in obtaining the improved results of the present invention.
When the silicon dioxide which is hydrophobic is combined with the lower alkyl α-cyanoacrylate, the hydrophilic properties of the resulting sealing material are substantially reduced, which increases the water-resisting qualities in oral cavities and prevents the deterioration of teeth. Favorable properties, such as the hardness and abrasion-resistant properties, are reinforced with silicon dioxide.
Because the ultra microfine particles are uniformly dispersed, the material is useful in reducing the residual strain of the resin on hardening and decreases the thermal expansion coefficient in the oral cavities after sealing and thereby relieves the influence of the internal stress of the sealing material. Accordingly, exfoliation, loss or leakage of the sealing material does not occur, and the adhesive strength to the teeth is maintained semipermanently. In the prior art compositions when the filler having a large particle size is combined with the resin in the sealing material, the abrasion-resistant properties were improved but the resinous properties were spoiled. This disadvantage is improved in the present invention.
The second material used in this invention is a di-lower alkyl formamide, which may be employed in admixture with the first material just prior to use to initiate polymerization of the lower alkyl α-cyanoacrylate. One to 20 parts, preferably 2 to 10 parts by weight of the di-loweralkyl formamide per 100 parts by weight of the first material is mixed with the first material. The thus obtained mixture may be employed within 2 to 3 minutes to 1 to 2 hours after mixing, which time may be controlled according to the amount of di-lower-alkyl formamide in the admixture. The polymerization rate may be regulated by adding a very small amount of water to the di-loweralkylformamide or by blowing carbon dioxide into the di-loweralkylformamide.
Di-loweralkylformamide acts as a catalyst in the anionic polymerization reaction of lower alkyl α-cyanoacrylate, which progresses slowly. In such slow polymerization, a polymer having a high degree of polymerization is obtained, which has lowered residual strain and elevated flexibility in comparison with polymers obtained by rapid polymerization. Although the shrinkage coefficient of the lower alkyl α-cyanoacrylate on polymerization is, in general, large, the influence of shrinkage after sealing is decreased in the present invention as contraction, which will occur on polymerization, is produced before sealing by adding a di-loweralkylformamide to the first material prior to sealing to initiate the polymerization. As a result, the sealing of pits and fissures in the teeth, and the adhesive strength between the sealing material and tooth were found to be stable, and the integrity of the seal is maintained for a long time.
The third material of this invention includes N, N-dimethyl-p-toluidine, N, N-dimethylaniline and N, N-diethylaniline, which are generally dissolved in ethanol, n-hexane or the like.
Preferably, the surfaces of the teeth to be treated are prepared by brushing with pumice, etching with acids such as phosphoric acid and citric acid, washing with water and air-dried.
In performing the sealing technique of the present invention using the described materials, the mixture of the first and second materials which begins to polymerize, is coated on the surfaces of the teeth pretreated as described above, with the tip of a small brush. Since the mixture of materials is thixotropic as mentioned earlier in spite of its high viscosity, homogeneous coating of the desired portions is possible and clinical processability is very excellent.
Immediately after the first and second materials are mixed, the teeth are covered with the mixture. The third material is then applied. Hardening of the surface of the sealing material occurs within 10 to 15 seconds and occlusion is made possible. However, in the inner portions of the sealing material, the polymerization proceeds slowly because of the presence of the di-loweralkylformamide and thereby the preferred polymer is obtained. The results obtained are excellent and the tooth surfaces are finely finished. Grinding of the occlusal surfaces is not required, except when the sealing is too high.
The coated sealant adheres firmly to teeth physically and chemically at the surfaces of the pits and fissures, and does not easily exfoliate, loosen or leak out.
Having generally described this invention, a further understanding can be obtained by reference to certain specific examples which are provided herein for purposes of illustration only and are not intended to be limiting unless otherwise specified.
After the pits and fissures of extracted human molar teeth were sealed according to the present process, they were exposed to severe conditions and were immersed alternately in 0.2% fuchsin aqueous solution at 4° C and 60° C, respectively for one minute. This procedure was repeated for 3 hours, and the teeth were tested.
As a result of the examination, it was found that no pigments penetrated the joining interfaces between the sealant and teeth, and the sealant was not stained at all. These results indicated that the sealant according to the present invention completely adhered to the teeth and exhibited good durability over a long time in oral cavities.
The adhesive strength of sealant to the enamel of teeth was tested in the following manner. After the labial surface of a bovine tooth was etched with acid, the tooth was coated with a mixture of the first and second materials of the sealant of the present invention. A round stick of Polymethacryl (6 mm diameter) was placed against the coated materials and the third material was applied onto the surface of the materials to harden the composition.
The coated tooth was immersed in water at 37° C for one week within 5 minutes after applying the third material, and thereafter the tensile strength was measured with a tensile testing machine and the adhesive strength per unit of area was calculated.
______________________________________
Sealants of this invention
Adhesive strength
______________________________________
Ethyl α-cyanoacrylate
100 parts
Aerosil R 972 10 parts 110 ± 20 Kg/cm.sup.2
Dimethylformamide 5 parts
n-Hexane solution containing 2%
of N,N-dimethyl-p-toluidine
______________________________________
Ethyl α-cyanoacrylate
100 parts
Aerosil R 972 5 parts 145 ± 30 Kg/cm.sup.2
Dimethylformamide 5 parts
n-Hexane solution containing 2%
of N,N-dimethyl-p-toluidine
______________________________________
Ethyl α-cyanoacrylate
100 parts
Aerosil OX 50 10 parts 133 ± 26 Kg/cm.sup.2
Dimethylformamide 5 parts
n-Hexane solution containing 2%
of N,N-dimethyl-p-toluidine
______________________________________
As can be seen from these results, the sealant of this invention adheres extremely well compared to the conventional sealants.
As mentioned above, the processability, water-resisting properties and the hardness of the composition of the present invention are improved by employing the combination of the first, second and third materials. Moreover, sealants having lowered residual strain and great flexibility are obtained as shrinkage on hardening is reduced and internal stress is relieved because of the combination of an ultra-microfine powder of silicon dioxide and the slow starting of the polymerization caused by the di-loweralkylformamide. Thus, great adhesive strength between the sealants and the enamel is maintained.
The first material: 7 percent Aerosil R 972 is mixed with ethyl α-cyanoacrylate.
The second material: Dimethylformamide.
The third material: n-Hexane solution containing 2%, N,N-dimethyl-p-toluidine.
Five percent of the second material was mixed with the first material as described above and then the resulting mixture was allowed to stand for 2 to 10 minutes, during which time the surfaces of the molar teeth of a patient were etched with 3 M phosphoric acid for 30 seconds, and washed with water. Moisture was removed from the teeth by a cotton roll and the teeth were air-dried. The mixture of the first and second materials as described above was coated onto the teeth surfaces by the tip of a small brush impregnated with the mixture. The mixture penetrated into the pits and fissures of the teeth. Then the third material was applied onto the teeth surfaces and allowed to stand for 5 to 15 seconds. It took about 2 minutes to treat the patient.
Having now fully described the invention, it will be apparent to one of ordinary skill in the art that many changes and modifications can be made thereto without departing from the spirit or scope of the invention as set forth herein.
Claims (1)
1. A method for preventing teeth from decaying by sealing pits and fissures of sound teeth, which comprises:
coating the surface of teeth with a mixture of a first material comprising a lower alkyl α-cyanoacrylate and ultra-microfine particles of silicon dioxide and a second material comprising a di-loweralkylformamide and then applying a third material of N,N-dimethyl-p-toluidine, N,N-dimethylaniline or N,N-diethylaniline onto the coated surface.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/657,585 US4012840A (en) | 1974-09-24 | 1976-02-12 | Adhesive pit and fissure sealant |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US50873374A | 1974-09-24 | 1974-09-24 | |
| US05/657,585 US4012840A (en) | 1974-09-24 | 1976-02-12 | Adhesive pit and fissure sealant |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US50873374A Division | 1974-09-24 | 1974-09-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4012840A true US4012840A (en) | 1977-03-22 |
Family
ID=27056285
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US05/657,585 Expired - Lifetime US4012840A (en) | 1974-09-24 | 1976-02-12 | Adhesive pit and fissure sealant |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US4012840A (en) |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4180913A (en) * | 1976-11-13 | 1980-01-01 | Lion Hamigaki Kabushiki Kaisha | α-Cyanoacrylate dental material and method of preparation |
| US4378213A (en) * | 1980-09-02 | 1983-03-29 | Mds Products Company, Inc. | Use of cyanoacrylate compounds for dental modeling |
| US4529384A (en) * | 1980-09-02 | 1985-07-16 | Mds Products, Inc. | Use of cyanoacrylate compounds for dental modeling |
| US5133957A (en) * | 1991-09-18 | 1992-07-28 | Bisco, Inc. | Composition and method for desensitizing dentin |
| US5955514A (en) * | 1993-04-19 | 1999-09-21 | Dentsply Research & Development Corp. | Dental composition and method |
| US5981620A (en) * | 1993-04-19 | 1999-11-09 | Dentsply Research & Development Corp. | Dental compounds, compositions, products and methods |
| US6391940B1 (en) | 1993-04-19 | 2002-05-21 | Dentsply Research & Development Corp. | Method and composition for adhering to metal dental structure |
| US6444725B1 (en) | 2000-01-21 | 2002-09-03 | 3M Innovative Properties Company | Color-changing dental compositions |
| US6528555B1 (en) | 2000-10-12 | 2003-03-04 | 3M Innovative Properties Company | Adhesive for use in the oral environment having color-changing capabilities |
| USD721813S1 (en) | 2013-10-23 | 2015-01-27 | Pinkband Dental Solutions, Inc. | Dental matrix band |
| USD721812S1 (en) | 2013-10-23 | 2015-01-27 | Pinkband Dental Solutions, Inc. | Dental matrix band |
| JP2021066670A (en) * | 2019-10-18 | 2021-04-30 | 宝禮 高槻 | Agent for oral cavity |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3518762A (en) * | 1965-10-29 | 1970-07-07 | Mitsuharu Takeuchi | Sealing materials useful in dental practice |
| US3540126A (en) * | 1968-07-16 | 1970-11-17 | Minnesota Mining & Mfg | Fluoroalkoxyalkyl 2 - cyanoacrylate compositions used in tooth treatment |
-
1976
- 1976-02-12 US US05/657,585 patent/US4012840A/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3518762A (en) * | 1965-10-29 | 1970-07-07 | Mitsuharu Takeuchi | Sealing materials useful in dental practice |
| US3540126A (en) * | 1968-07-16 | 1970-11-17 | Minnesota Mining & Mfg | Fluoroalkoxyalkyl 2 - cyanoacrylate compositions used in tooth treatment |
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4180913A (en) * | 1976-11-13 | 1980-01-01 | Lion Hamigaki Kabushiki Kaisha | α-Cyanoacrylate dental material and method of preparation |
| US4378213A (en) * | 1980-09-02 | 1983-03-29 | Mds Products Company, Inc. | Use of cyanoacrylate compounds for dental modeling |
| US4529384A (en) * | 1980-09-02 | 1985-07-16 | Mds Products, Inc. | Use of cyanoacrylate compounds for dental modeling |
| US5133957A (en) * | 1991-09-18 | 1992-07-28 | Bisco, Inc. | Composition and method for desensitizing dentin |
| US6391940B1 (en) | 1993-04-19 | 2002-05-21 | Dentsply Research & Development Corp. | Method and composition for adhering to metal dental structure |
| US5981620A (en) * | 1993-04-19 | 1999-11-09 | Dentsply Research & Development Corp. | Dental compounds, compositions, products and methods |
| US5955514A (en) * | 1993-04-19 | 1999-09-21 | Dentsply Research & Development Corp. | Dental composition and method |
| US6500879B1 (en) | 1993-04-19 | 2002-12-31 | Dentsply Research & Development Corp. | Dental composition and method |
| US6444725B1 (en) | 2000-01-21 | 2002-09-03 | 3M Innovative Properties Company | Color-changing dental compositions |
| US6528555B1 (en) | 2000-10-12 | 2003-03-04 | 3M Innovative Properties Company | Adhesive for use in the oral environment having color-changing capabilities |
| USD721813S1 (en) | 2013-10-23 | 2015-01-27 | Pinkband Dental Solutions, Inc. | Dental matrix band |
| USD721812S1 (en) | 2013-10-23 | 2015-01-27 | Pinkband Dental Solutions, Inc. | Dental matrix band |
| JP2021066670A (en) * | 2019-10-18 | 2021-04-30 | 宝禮 高槻 | Agent for oral cavity |
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